ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.3204T>G (p.Ser1068=)

dbSNP: rs2073312963
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001188303 SCV001355326 likely benign Cardiomyopathy 2020-01-15 criteria provided, single submitter clinical testing

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